Chapter 13 THE RESPIRATORY CHAIN AND OXIDATIVE PHOSPHORYLATION Flashcards

1
Q

Respiration is coupled to the generation of the high-energy intermediate, ATP, by ____

A

oxidative phosphorylation

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2
Q

part of mitochondria that is permeable to most metabolites

A

Outer membrane

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3
Q

part of mitochondria that is selectively permeable

A

Inner membrane

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4
Q
  • material inside the mitochondria,

- contains enzymes, mtDNA, mtRNA, mitochondrial ribosomes

A

Matrix

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5
Q

The outer membrane is characterized by the presence of various enzymes including ____ and ____

A

acyl-CoA synthetase;

glycerol phosphate acyltransferase

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6
Q

enzymes that are found in the intermembrane space of mitochondria

A

adenylyl kinase and creatine kinase

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7
Q

is concentrated in the inner membrane together with the enzymes of the respiratory chain, ATP synthase, and various membrane transporters

A

phospholipid cardiolipin

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8
Q
  • are important components of Complexes I and II
A

Flavoproteins

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9
Q
  • are found in Complexes I, II, and III

- may contain one, two, or four Fe atoms linked to inorganic sulfur atoms and/or via cysteine-SH groups to the protein

A

Iron-sulfur proteins (nonheme iron proteins, Fe-S)

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10
Q

is a large L-shaped multisubunit protein that catalyzes electron transfer from NADH to Q, coupled with the transfer of four H+ across the membrane

A

NADH-Q oxidoreductase or Complex I

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11
Q

an unusual Fe-S in which one of the Fe atoms is linked to two histidine residues rather than two cysteine residues

A

Rieske Fe-S

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12
Q

The flow of electrons through the respiratory chain generates ATP by the process of

A

oxidative phosphorylation

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13
Q

postulates that the two processes are coupled by a proton gradient across the inner mitochondrial membrane so that the proton motive force caused by the electrochemical potential difference (negative on the matrix side) drives the mechanism of ATP synthesis

A

chemiosmotic theory

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14
Q

oxidation cannot proceed via the respiratory chain without concomitant phosphorylation of ADP

A

because oxidation and phosphorylation are tightly coupled

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15
Q

inhibit electron transport via Complex I by blocking the transfer from Fe-S to Q

A

Barbiturates

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16
Q

inhibit the respiratory chain at Complex III

A

Antimycin A and dimercaprol

17
Q

States of Respiratory Control

A

State 1 - Availability of ADP and substrate
State 2 - Availability of substrate only
State 3 - The capacity of the respiratory chain itself, when all substrates and components are present in saturating amounts
State 4 - Availability of ADP only
State 5 - Availability of oxygen only

18
Q

inhibit Complex IV and can therefore totally arrest respiration

A

H2S, carbon monoxide, and cyanide

19
Q

is a competitive inhibitor of Complex II

A

Malonate

20
Q

inhibits oxidative phosphorylation by inhibiting the transporter of ADP into and ATP out of the mitochondrion

A

Atractyloside

21
Q

completely blocks oxidation and phosphorylation by blocking the flow of protons through ATP synthase

A

Oligomycin

22
Q

dissociate oxidation in the respiratory chain from phosphorylation

A

Uncouplers

23
Q

(or the uncoupling protein) is a physiological uncoupler found in brown adipose tissue that functions to generate body heat, particularly for the newborn and during hibernation in anima

A

Thermoginin

24
Q

involving transporter proteins that span the membrane are present in the membrane for exchange of anions against OH− ions and cations against H+ ions

A

Exchange diffusion systems

25
Q

are transported into mitochondria via the carnitine system

A

Long-chain fatty acids

26
Q

are lipophilic molecules that complex specific cations

and facilitate their transport through biologic membranes

A

Ionophores

27
Q

augments the functions of creatine phosphate as an energy buffer by acting as a dynamic system for transfer of high-energy phosphate from mitochondria in active tissues such as heart and skeletal muscle

A

creatine phosphate shuttle

28
Q

is found in the mitochondrial intermembrane space, catalyzing the transfer of high-energy phosphate to creatine from ATP emerging from the adenine nucleotide transporter

A

Isoenzyme of creatine kinase (CKm)

29
Q

involves severe diminution

or absence of most oxidoreductases of the respiratory chain

A

fatal infantile mitochondrial myopathy and renal dysfunction

30
Q

is an inherited condition due to NADH-Q oxidoreductase (Complex I) or cytochrome oxidase (Complex IV) deficiency

A

MELAS (mitochondrial encephalopathy, lactic acidosis, and

stroke)

31
Q
  • Energy from oxidation of components in the respiratory chain is couples with translocation of hydrogen ions
  • hydrogen is moved from the inside to the outside of the inner mitochondrial membrane –> accumulates in the intermembranous space
A

Mitchell’s Chemiosmotic Theory

32
Q

Inhibitors of ETC in Compex I

A

Amytal, Rotenone

33
Q

Inhibitors of ETC in Compex II

A

Malonate

34
Q

Inhibitors of ETC in Compex III

A

Anitimycin A, Dimercaprol

35
Q

Inhibitors of ETC in Compex IV

A

Hydrogen Sulfide, Carbon Monoxide, Cyanide, Sodium Azide

36
Q

Inhibitors of ETC in Compex V

A

Oligomycin